父源性15q11q13片段缺失所致Prader-Willi综合征1型
ORPHA:177901· ICD-10 Q87.1· Prader-Willi syndrome due to paternal deletion of 15q11q13 type 1
- 遗传方式
- Autosomal dominant
- 发病年龄
- Antenatal, Neonatal
ORPHA:177901· ICD-10 Q87.1· Prader-Willi syndrome due to paternal deletion of 15q11q13 type 1